Online Workshop: Basics of Regulatory Affairs in MedTech
Anleitung
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Introduction to Regulatory Affairs in Medtech
Date 29 - 30 June and 1 July, 2021
Time 10.00 - 12.00 CEST
Place Online - Registration closed Cost The workshop is free of charge This training provides you with the basics of regulatory affairs in MedTech with the focus on MDR and IVDR (Medical Devices and In-Vitro Diagnostic Medical Devices Regulation). Get an overview of the regulatory landscape, hear about the basic concepts and principles and get insights into the necessary steps but also pitfalls when bringing a MedTech product to the market. Discuss with the experts.
Target Audience
- Researchers in the field of translational medicine
- Employees from spin-offs, start-ups and SMEs, who intend to bring a product to the market
- Employees from companies interested in getting an overview on regulatory affairs
- Investors in medical devices who would like to understand risks and opportunities regarding the evolving regulatory framework in EU
For more information please see program flyer
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Registration closed
Participants will receive the login information for the webinar by email on 28th June 2021.
A certificate of attendance will be issued for participants that participated on all three days.
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Organizer & Partner
Kontakt
Amt für Wirtschaft und Arbeit – Standortförderung
